ClinVar Miner

List of variants in gene FNDC3A reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001079673.2(FNDC3A):c.3320G>A (p.Ser1107Asn) rs199704841 0.00017
NM_001079673.2(FNDC3A):c.355C>G (p.Leu119Val) rs772925881 0.00015
NM_001079673.2(FNDC3A):c.2053C>T (p.Pro685Ser) rs375633208 0.00009
NM_001079673.2(FNDC3A):c.3494G>A (p.Arg1165Gln) rs143452842 0.00009
NM_001079673.2(FNDC3A):c.1366G>C (p.Glu456Gln) rs201568850 0.00006
NM_001079673.2(FNDC3A):c.3310C>T (p.Arg1104Trp) rs150282972 0.00006
NM_001079673.2(FNDC3A):c.1142A>G (p.Asn381Ser) rs754475479 0.00005
NM_001079673.2(FNDC3A):c.2590G>A (p.Asp864Asn) rs144439368 0.00005
NM_001079673.2(FNDC3A):c.679G>C (p.Ala227Pro) rs373846216 0.00005
NM_001079673.2(FNDC3A):c.1378T>C (p.Tyr460His) rs192690498 0.00003
NM_001079673.2(FNDC3A):c.165G>C (p.Gln55His) rs758085923 0.00003
NM_001079673.2(FNDC3A):c.3206G>C (p.Cys1069Ser) rs544542712 0.00003
NM_001079673.2(FNDC3A):c.496C>T (p.His166Tyr) rs373831224 0.00003
NM_001079673.2(FNDC3A):c.2210C>T (p.Ala737Val) rs763284396 0.00002
NM_001079673.2(FNDC3A):c.46A>G (p.Ser16Gly) rs776807608 0.00002
NM_001079673.2(FNDC3A):c.481G>A (p.Gly161Arg) rs763226463 0.00002
NM_001079673.2(FNDC3A):c.769G>A (p.Glu257Lys) rs374067441 0.00002
NM_001079673.2(FNDC3A):c.1136T>C (p.Ile379Thr) rs1884607527 0.00001
NM_001079673.2(FNDC3A):c.1178C>T (p.Ala393Val) rs767890755 0.00001
NM_001079673.2(FNDC3A):c.1507T>G (p.Leu503Val) rs772709062 0.00001
NM_001079673.2(FNDC3A):c.1712C>T (p.Ser571Leu) rs375462764 0.00001
NM_001079673.2(FNDC3A):c.2100A>C (p.Glu700Asp) rs760474446 0.00001
NM_001079673.2(FNDC3A):c.3122C>G (p.Thr1041Ser) rs143582787 0.00001
NM_001079673.2(FNDC3A):c.3548T>G (p.Phe1183Cys) rs2547031705 0.00001
NM_001079673.2(FNDC3A):c.536C>G (p.Ser179Cys) rs1882358282 0.00001
NM_001079673.2(FNDC3A):c.881A>G (p.Asn294Ser) rs765196205 0.00001
NM_001079673.2(FNDC3A):c.1006G>A (p.Asp336Asn) rs768686708
NM_001079673.2(FNDC3A):c.1144C>T (p.Arg382Trp) rs367707181
NM_001079673.2(FNDC3A):c.1145G>A (p.Arg382Gln)
NM_001079673.2(FNDC3A):c.115G>A (p.Val39Ile) rs2541594145
NM_001079673.2(FNDC3A):c.1331C>T (p.Ser444Leu)
NM_001079673.2(FNDC3A):c.1579G>T (p.Val527Leu) rs1433784816
NM_001079673.2(FNDC3A):c.1862G>A (p.Arg621Lys)
NM_001079673.2(FNDC3A):c.1879C>G (p.Arg627Gly) rs772603743
NM_001079673.2(FNDC3A):c.1910G>A (p.Arg637Gln)
NM_001079673.2(FNDC3A):c.1927G>T (p.Asp643Tyr)
NM_001079673.2(FNDC3A):c.1936C>G (p.Gln646Glu)
NM_001079673.2(FNDC3A):c.2107C>T (p.Pro703Ser)
NM_001079673.2(FNDC3A):c.2130A>T (p.Arg710Ser)
NM_001079673.2(FNDC3A):c.2168G>A (p.Ser723Asn)
NM_001079673.2(FNDC3A):c.2189C>T (p.Thr730Ile)
NM_001079673.2(FNDC3A):c.2206C>T (p.Arg736Cys) rs771506910
NM_001079673.2(FNDC3A):c.2252A>G (p.Asp751Gly)
NM_001079673.2(FNDC3A):c.2275C>A (p.Pro759Thr)
NM_001079673.2(FNDC3A):c.2289G>C (p.Lys763Asn) rs752465260
NM_001079673.2(FNDC3A):c.2366T>C (p.Val789Ala) rs1886223272
NM_001079673.2(FNDC3A):c.244G>A (p.Ala82Thr) rs2541665938
NM_001079673.2(FNDC3A):c.2452G>A (p.Gly818Arg)
NM_001079673.2(FNDC3A):c.2509G>A (p.Ala837Thr)
NM_001079673.2(FNDC3A):c.2549C>T (p.Pro850Leu)
NM_001079673.2(FNDC3A):c.2681C>T (p.Ala894Val)
NM_001079673.2(FNDC3A):c.2750A>G (p.Asn917Ser)
NM_001079673.2(FNDC3A):c.2751T>G (p.Asn917Lys) rs2547023092
NM_001079673.2(FNDC3A):c.2816T>C (p.Phe939Ser) rs2547023331
NM_001079673.2(FNDC3A):c.2944G>A (p.Asp982Asn)
NM_001079673.2(FNDC3A):c.3067A>C (p.Ile1023Leu)
NM_001079673.2(FNDC3A):c.3089G>C (p.Gly1030Ala)
NM_001079673.2(FNDC3A):c.3113A>G (p.Tyr1038Cys) rs747543589
NM_001079673.2(FNDC3A):c.3115A>G (p.Ile1039Val)
NM_001079673.2(FNDC3A):c.3425T>C (p.Leu1142Pro) rs1313078027
NM_001079673.2(FNDC3A):c.3506G>A (p.Ser1169Asn) rs2547031627
NM_001079673.2(FNDC3A):c.404A>C (p.His135Pro) rs762348761
NM_001079673.2(FNDC3A):c.418G>A (p.Val140Met)
NM_001079673.2(FNDC3A):c.499T>G (p.Ser167Ala) rs772136953
NM_001079673.2(FNDC3A):c.538A>T (p.Ser180Cys) rs759935299
NM_001079673.2(FNDC3A):c.53T>C (p.Ile18Thr)
NM_001079673.2(FNDC3A):c.578G>T (p.Arg193Leu)
NM_001079673.2(FNDC3A):c.584G>A (p.Gly195Glu) rs2541712314
NM_001079673.2(FNDC3A):c.59T>G (p.Leu20Arg) rs764499260
NM_001079673.2(FNDC3A):c.766G>C (p.Asp256His) rs768845610
NM_001079673.2(FNDC3A):c.821C>T (p.Ala274Val)
NM_001079673.2(FNDC3A):c.826G>A (p.Asp276Asn)
NM_001079673.2(FNDC3A):c.841A>G (p.Thr281Ala)
NM_001079673.2(FNDC3A):c.965A>G (p.Lys322Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.